Chemistry of 5-oxodihydroisoxazoles .18. Synthesis of oxazoles by the photolysis and pyrolysis of 2-acyl-5-oxo-2,5-dihydroisoxazoles

被引:42
作者
Prager, RH
Smith, JA
Weber, B
Williams, CM
机构
[1] Department of Chemistry, Flinders University of South Australia, Adelaide, SA 5001
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1997年 / 17期
关键词
D O I
10.1039/a700134g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
N-Acylisoxazol-5-ones lose carbon dioxide under photochemical and thermal conditions affording iminocarbenes which undergo intramolecular cyclisation through the oxygen of the acyl group to give oxazoles. Under photochemical conditions those acylisoxazolones with electron withdrawing groups at C-4 usually give high yields of oxazoles, while those with electron donating groups at C-4 give only poor yields: the reverse is observed under thermal conditions.
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页码:2665 / 2672
页数:8
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